This request is based on a comment from the "Unipro UGENE NGS pipelines and components for variant calling, RNA-seq and ChIP-seq data analyses" paper reviewer.
This would be more beneficial for the biologist and also for easy adaption if authors can Include ready to use best practices workflows. For example:
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4. Structural variants analysis workflow for both DNASeq and RNASeq (gene-fusions)
- relates to
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UGENE-3547 Integrate other variant calling workflows
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- Closed
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- Closed
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- Closed
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